Working Group 6: Educational Training of Research Staff Involved in Paediatric Clinical Trials / GCP Training across multispecialty and countries
Working Group 6 : GCP Training Across Multi-specialties and Countries Chair: Gareth Veal Membership: Salma Malik, Mary Costello, Susan Macfarlane, Pirkko Lepola, Adriana Ceci, Florence Bosco Objectives: Training of research nurses who conduct clinical trials: models, needs and current gaps across different specialties and countries
Purpose: To review the current requirements, level and consistency of training received by research nurses involved in paediatric clinical trials across different European countries. What does this training involve and how frequently is it provided? To identify potential gaps in training and the purported needs of research nurses currently involved in paediatric trials. How might these gaps be filled through the development of optimal research nurse training models? To assess variation in the role and scope of research nurse activities across European countries and specialties. What level of responsibility is given in terms of taking consent, prescribing drugs for CTIMPs, etc.?
Key Tasks, Tim efram es and Outputs • To design a questionnaire-based study to allow the generation of information on what research nurse training models currently exist, what training is currently given and what gaps there may be in training across different specialties and countries. • An initial draft of the questionnaire will be developed and finalised by the working group by the end of November, 2015. • The initial draft will be circulated to Enpr-EMA networks for comments in December, 2015. • To assemble a list of research nurse groups/ networks and contact details covering a wide range of European countries and specialties. • To assess the most effective method of carrying out the questionnaire-based survey across the groups defined above. • To obtain and collate the information received, share the data with the Enpr-EMA networks (May, 2016) and review the potential for publication.
Areas of focus for questionnaire: • Area of work (specialties, age range, etc) • Level of experience • Training received and frequency • Additional training requirements? • Form of training received • GCP certified training? • Roles of research nurse (clinical trial-related)
Summary of data obtained: • Total of 28 organisations identified for circulation of questionnaire study • Countries: UK, Ireland, France, Switzerland, Finland, Norway, Sweden, Denmark, Netherlands, Spain, Germany, Italy • Specialties: Oncology, haematology, neonatal (majority ‘multiple’) • Link to questionnaires sent to points of contact for each organisation between 12-13 th April, 2016. • Translation of questionnaire into French for organisations in France • Completed questionnaires received to date: 201
Paediatric Specialties
Age of Children
Research Nurse Experience
Level of Training Received 1/3 research nurses felt that they would benefit from additional training. Specific areas of need identified: • IT training / clinical trial setup / specialist skills for clinical trials / sample handling / finance / research governance
Specifics of Training Received
Frequency of Training Received
Research Nurse Activities Ethics Applications Development of PIS Development of Consent Forms Trial Amendments Development of Trial CRFs
Participation in CTIMPs • 84% of research nurses completing questionnaire participate in CTIMPs • 57% of research nurses participate in Phase I/II trials Processing Samples Sample Transport Taking Consent Prescribing IMPs Administration of IMPs Training / Education for Patients
Questionnaire Responses by Country
Immediate and Future Plans: • Identification of organisations for circulation of questionnaire study in countries currently under-represented in dataset obtained • Analysis of data obtained • Publication of study data in appropriate journal with data summary and link to publication through EnprEMA website • Potential impact of findings on future research nurse training
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